HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598547Generated: October 25, 2026
Potassium Carbonate → (RS)-4,5-Difluoro-2-piperidin-2-ylmethyl-1H-benzoimidazole
https://huagongshe.com/reaction/598547
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,4-Difluorobenzene-1,2-diamine | HCID 2736753 | — |
| Reactant | 1-Boc-2-Piperidineacetic Acid | HCID 5058536 | — |
| Product | (RS)-4,5-Difluoro-2-piperidin-2-ylmethyl-1H-benzoimidazole | HCID 17973676 | 62% |
Reaction Steps
A mixture of 2-carboxymethyl-piperidine-1-carboxylic acid tert-butyl ester (Beckett et al, J. Med. Chem., 563, 1969) (6.72 g, 28 mmol) and 3,4-difluoro-benzene-1,2-diamine (4.00 g, 28 mmol) in polyphosphoric acid (130 g) was heated at 140° C. for 7.5 h. The cooled reaction mixture was poured onto excess solid potassium carbonate and crushed ice. The resulting basic, aqueous solution was extracted with ethyl acetate (2×) and the combined organics were washed with brine, dried (Na2SO4) and the solvent removed in vacuo. The residue was triturated with diethyl ether, ethyl acetate and pentane to afford the title compound as a white solid (4.29 g, 62%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897618B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-3e465382713242fe8c5dc548afbec584 |
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| Source note | uspto-grants-2011_03 |
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